Evidence map›Paper›PMID 33495447›Full record

ArticleCell death & disease2021

SCA-1 micro-heterogeneity in the fate decision of dystrophic fibro/adipogenic progenitors.

Giulio Giuliani, Simone Vumbaca, Claudia Fuoco, Cesare Gargioli, Ezio Giorda, Giorgia Massacci, Alessandro Palma, Alessio Reggio, Federica Riccio, Marco Rosina and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 39 citations in OpenAlex.

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  13. MuSCs and IPCs: roles in skeletal muscle homeostasis, aging and injury.Cellular and molecular life sciences : CMLS · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Giulio GiulianiDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy. g.giulianigiulio@gmail.com.ORCID 0000-0002-4648-0076
Simone VumbacaDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0003-1940-3355
Claudia FuocoDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Cesare GargioliDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0003-1742-3969
Ezio GiordaCore Facilities, Bambino Gesù Children's Hospital - IRCCS, Rome, Italy.
Giorgia MassacciDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0003-3223-6547
Alessandro PalmaDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0003-1300-5479
Alessio ReggioDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0001-5333-7502
Federica RiccioDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Marco RosinaDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0003-0952-1710
Maria VinciDepartment of Onco-haematology, Cell and Gene Therapy, Bambino Gesù Children's Hospital - IRCCS, Rome, Italy.ORCID 0000-0002-7952-6771
Luisa CastagnoliDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Gianni CesareniDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0002-9528-6018
University of Rome Tor Vergata · ITBambino Gesù Children's Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The term micro-heterogeneity refers to non-genetic cell to cell variability observed in a bell-shaped distribution of the expression of a trait within a population. The contribution of micro-heterogeneity to physiology and pathology remains largely uncharacterised. To address such an issue, we investigated the impact of heterogeneity in skeletal muscle fibro/adipogenic progenitors (FAPs) isolated from an animal model of Duchenne muscular dystrophy (DMD), the mdx mouse. FAPs play an essential role in muscle homoeostasis. However, in pathological conditions or ageing, they are the source of intramuscular infiltrations of fibrotic or adipose tissue. By applying a multiplex flow cytometry assay, we characterised and purified from mdx muscles two FAP cell states expressing different levels of SCA-1. The two cell states are morphologically identical and repopulate each other after several growth cycles. However, they differ in their in vitro behaviour. Cells expressing higher levels of SCA-1 (SCA1-High-FAPs) differentiate more readily into adipocytes while, when exposed to a fibrogenic stimulation, increase the expression of Col1a1 and Timp1 mRNA. A transcriptomic analysis confirmed the adipogenic propensity of SCA1-High-FAPs. In addition, SCA1-High-FAPs proliferate more extensively ex vivo and display more proliferating cells in dystrophic muscles in comparison to SCA1-Low-FAPs. Adipogenesis of both FAP cell states is inhibited in vitro by leucocytes from young dystrophic mice, while leucocytes isolated from aged dystrophic mice are less effective in limiting the adipogenesis of SCA1-High-FAPs suggesting a differential regulatory effect of the microenvironment on micro-heterogeneity. Our data suggest that FAP micro-heterogeneity is modulated in pathological conditions and that this heterogeneity in turn may impact on the behaviour of interstitial mesenchymal cells in genetic diseases.

Indexed as

AdipogenesisAnimalsAntigens, LyCell DifferentiationMembrane ProteinsMesenchymal Stem CellsMiceAntigens, LyLy6a protein, mouseMembrane Proteins

Identifiers

PMID33495447
PMCPMC7835386
OpenAlexW3123128175

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.